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The Journal of Immunology, 2005, 175: 7103-7107.
Copyright © 2005 by The American Association of Immunologists


CUTTING EDGE

Cutting Edge: The Development of IL-4-Producing B Cells (B Effector 2 Cells) Is Controlled by IL-4, IL-4 Receptor {alpha}, and Th2 Cells1

David P. Harris2, Stephen Goodrich, Katja Mohrs, Markus Mohrs and Frances E. Lund3

Trudeau Institute, Saranac Lake, NY 12983

Although IL-4-producing B cells (B effector 2 cells) are found following infection and immunization, the signals regulating IL-4 production by Be2 cells are unknown. We show that culturing naive B cells with Th2 cells induces up-regulation of IL-4 in the B cells with a concomitant down-regulation of T-bet, IL-12R{beta}2, and IFN-{gamma}. Up-regulation of IL-4 in the Be2 cells is dependent on both T cells and IL-4 as IL-4R{alpha}-deficient B cells primed with Th2 cells did not transcribe IL-4, and B cells primed in the presence of IL-4-deficient Th2 cells produced IFN-{gamma} instead of IL-4. Likewise, the in vivo development of IL-4-expressing B cells in a nematode infection model was dependent on both T cells and IL-4R{alpha}-mediated signals. Thus, the differentiation of naive B cells into IL-4-expressing Be2 cells is regulated by a combination of T cell-dependent signals and the cytokine environment and this process is critically dependent upon the IL-4/IL-4R signaling pathway.


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The JI 2005 175: 7065-7066. [Full Text]  



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